Long Reads.
Less Wait.
Nanopore Sequencing
Up to 40% off.
Data in as Fast as 10 Working Days.
T&C apply. Offer valid till 31st August 2026.
Whether you're exploring structural variants and DNA modifications (5mC, 5hmC) from a single sequencing workflow or generating high-quality genome assemblies, our expanded sequencing capacity in Singapore helps you move from samples to insights faster.
Comprehensive
Bioinformatics Support
Go beyond sequencing with our integrated bioinformatics support that helps you uncover meaningful biological insights. Our key analysis services include:
- Structural Variant (SV) Discovery for accurate detection of complex genomic alterations
- Direct Base Modification Calling (e.g., 5mC, 5hmC) without additional experimental workflows
- High-Quality De Novo Genome Assembly, including near T2T-level assemblies, with customized solutions designed to meet specific project goals and genome complexities
Which Long-Read Platform Fits Your Research?
As a multi-platform sequencing provider, we support both Nanopore and PacBio technologies. The most suitable platform depends on your research objectives, data requirements, and budget considerations.
Talk to a Novogene representative
| Platform Parameters | Oxford Nanopore Technologies | PacBio |
|---|---|---|
| Read length | 10–100 kb | 15–20 kb |
| Average Read Accuracy | ~ Q20 | ≥ Q30 |
| Direct modification detection | 5mC, 5hmC | |
| Structural Variants (SV) |
✓ Including accurate resolution of repetitive regions and large structural variants (spanning tens to hundreds of kilobases) |
✓ |
| Copy Number Variants (CNV) | ✓ | ✓ |
| Single Nucleotide Polymorphisms (SNP) | ✓ | |
| Short Tandem Repeats (STR) | ✓ | |
| De novo Assembly | Telomere-to-Telomere (T2T) Level | Chromosome Level |
| Cost | $ | $$ |
Why Nanopore Sequencing?
Nanopore sequencing enables direct detection of base modifications (including 5mC and 5hmC) alongside primary sequence identification, without the need for bisulfite conversion or antibody enrichment.
Its long-read capability (spanning tens to hundreds of kilobases) allows accurate resolution of repetitive regions and large structural variants — such as insertions, deletions, inversions, and duplications — that are often missed by short-read sequencing technologies.
This capability also supports telomere-to-telomere (T2T) genome assembly, unlocking critical applications including centromere and telomere biology, discovery of structural variants in cancer genomes, and the construction of complete reference genomes for evolutionary studies.
Request Promotional Pricing
Complete the form below and our team will contact you to discuss your project requirements and promotional eligibility.
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Terms and Conditions
- To qualify for the promotion, project quotations, purchase orders, and physical samples must be received by 31 August 2026.
- The promotion applies to orders of ≥ 2 flow cells, with a minimum sample number of 1.
- Promotional pricing includes library preparation for one sample and sequencing on one flow cell. Additional library preparation charges will apply for projects requiring pooling of multiple samples into a single flow cell.
- Turnaround time is calculated from Novogene’s receipt of library preparation confirmation. Actual turnaround time may vary, particularly for multi-sample projects. Please contact your sales representative for further details.
- This promotion is exclusively available to clients in Africa, Australia, New Zealand, Korea, Middle East and Southeast Asia.
- Terms and conditions are subject to change without prior notice. Additional restrictions may apply.
About Novogene
Novogene is a pioneer in applying cutting-edge molecular biology technology and high-performance computing to research in the fields of life science and human health. Our vision is to continue as a global leader in the delivery of genomics services and solutions. With one of the largest sequencing capacities in the world, we utilise our deep scientific knowledge, first-class customer service and unsurpassed data quality to help clients realise their research goals in the rapidly evolving world of genomics. Novogene is committed to become your trusted genomics partner.
For more information, visit novogene.com/amea-en
© 2026 Novogene Co., Ltd. All Rights Reserved.
For Research Use Only. Not for Clinical Diagnostic Use.
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